1218790-05-6 Usage
Description
2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is an organic compound that serves as a key building block in the synthesis of various chemical compounds. It is characterized by its unique molecular structure, which includes a chloro group at the 2nd position, a trifluoromethyl group at the 6th position, and a boronic acid pinacol ester group at the 4th position of the pyridine ring. 2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is known for its reactivity and versatility in chemical reactions, making it a valuable intermediate in the development of new molecules with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties, such as novel drugs for the treatment of various diseases and disorders.
Used in Chemical Research:
In the field of chemical research, 2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is utilized as a versatile building block for the synthesis of complex organic molecules. Its reactivity and compatibility with various reaction conditions make it an ideal candidate for exploring new chemical pathways and discovering innovative molecular structures.
Used in Material Science:
2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is also employed in the field of material science, where it is used as a precursor for the development of advanced materials with unique properties. These materials may find applications in various industries, such as electronics, aerospace, and automotive, where high-performance materials are in demand.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloro-6-(trifluoromethyl)pyridine-4-boronic acid pinacol ester is used as a starting material for the synthesis of novel agrochemicals, such as pesticides and herbicides. Its unique structure allows for the development of new compounds with improved efficacy and selectivity, leading to more effective and environmentally friendly solutions for agricultural challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 1218790-05-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,7,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1218790-05:
(9*1)+(8*2)+(7*1)+(6*8)+(5*7)+(4*9)+(3*0)+(2*0)+(1*5)=156
156 % 10 = 6
So 1218790-05-6 is a valid CAS Registry Number.
1218790-05-6Relevant articles and documents
SUBSTITUTED ARYL COMPOUND AND PREPARATION METHOD THEREFOR AND USE THEREOF
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Paragraph 0197-0198; 0201, (2021/11/04)
The present application relates to a substituted aryl compound or a pharmaceutically acceptable salt, a stereoisomer, a polymorph, a solvate, a N-oxide, an isotope-labeled compound, a metabolite or a prodrug thereof, and a preparation method therefor and use thereof, also relates to a pharmaceutical composition containing the compound and a therapeutic use thereof. The compound or a pharmaceutical composition thereof can inhibit the activity of adenosine A2a receptor, and can be used for treating or preventing a disease related to adenosine A2a receptor, especially for treating a tumor.
Microwave-assisted, Ir-catalyzed aromatic C-H borylation
Zeqing, Li,Zhibin, Liang,Yuqiang, Wang,Pei, Yu
, p. 1917 - 1926 (2013/06/05)
One-step conversions of 1,3-disubstituted benzenes to aryl boronates and 2,6-disubstituted pyridines to heteroaryl boronates are described. Microwave heating was used for all reactions. [(COD)Ir(μ-OMe)]2 and 4,4′-di-tert-butyl-2,2′-bipyridine w
